Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Duplication | NM_024675.4(PALB2):c.1652dup (p.Tyr551Ter) | PALB2 | Pathogenic | 16 | 23646214 | 23646215 | A | AT | criteria provided, single submitter | - |
single nucleotide variant | NM_024675.4(PALB2):c.778C>T (p.Gln260Ter) | PALB2 | Pathogenic | 16 | 23647089 | 23647089 | G | A | criteria provided, single submitter | - |
Deletion | NC_000016.10:g.(?_23603449)_(23626407_?)del | PALB2 | Pathogenic | 16 | 23614770 | 23637728 | na | na | criteria provided, single submitter | - |
Deletion | NC_000016.10:g.(?_23626226)_(23630479_?)del | PALB2 | Pathogenic | 16 | 23637547 | 23641800 | na | na | criteria provided, single submitter | - |
single nucleotide variant | NM_024675.4(PALB2):c.3340C>T (p.Gln1114Ter) | PALB2 | Pathogenic | 16 | 23619195 | 23619195 | G | A | criteria provided, multiple submitters, no conflicts | - |
Duplication | NM_024675.4(PALB2):c.3008dup (p.Asn1003fs) | PALB2 | Pathogenic | 16 | 23632787 | 23632788 | G | GT | criteria provided, single submitter | - |
Duplication | NM_024675.4(PALB2):c.1212dup (p.Pro405fs) | PALB2 | Pathogenic | 16 | 23646654 | 23646655 | G | GA | criteria provided, single submitter | - |
Deletion | NM_024675.4(PALB2):c.1152del (p.Ala385fs) | PALB2 | Pathogenic | 16 | 23646715 | 23646715 | CT | C | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_024675.4(PALB2):c.995_996del (p.Leu332fs) | PALB2 | Pathogenic | 16 | 23646871 | 23646872 | TGA | T | criteria provided, single submitter | - |
Deletion | NM_024675.4(PALB2):c.532del (p.Glu178fs) | PALB2 | Pathogenic | 16 | 23647335 | 23647335 | TC | T | reviewed by expert panel | - |